Canonical Allele Identifier: CA5716577
Gene: BAG3 HGNC NCBI

Linked Data

ClinVar Variation Id: 471800
ClinVar RCV Id: RCV000554070
dbSNP Id: rs777325497
ExAC: 10:121436644 G / T
gnomAD v2: 10-121436644-G-T
gnomAD v3: 10-119677132-G-T
gnomAD v4: 10-119677132-G-T
MyVariant Identifiers: chr10:g.121436644G>T (hg19) chr10:g.119677132G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119677132G>T , CM000672.2:g.119677132G>T GRCh38
NC_000010.10:g.121436644G>T , CM000672.1:g.121436644G>T GRCh37
NC_000010.9:g.121426634G>T NCBI36
NG_016125.1:g.30763G>T , LRG_742:g.30763G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1578G>T MANE Select ENSP00000358081.4:p.Glu526Asp
ENST00000369085.7:c.1578G>T ENSP00000358081.3:p.Glu526Asp
NM_004281.3:c.1578G>T , LRG_742t1:c.1578G>T NP_004272.2:p.Glu526Asp
XM_005270287.1:c.1575G>T XP_005270344.1:p.Glu525Asp
XM_005270287.2:c.1575G>T XP_005270344.1:p.Glu525Asp
NM_004281.4:c.1578G>T MANE Select NP_004272.2:p.Glu526Asp
Search 100 bp 5'
Search 100 bp 3'